Katalyst Surgical, Llc: Forceps, Ophthalmic
Recall Summary Katalyst Surgical is recalling DEX Ophthalmic Tissue Forceps (model DVF4005-23) used in eye surgery due to incorrect instructions for use. The forceps were distributed nationwide in the US and in Peru, Argentina, South Korea, Japan, and France. This is classified as a Class I recall, the most serious category.
- Recalling firm
- Katalyst Surgical, LLC
- Product
- DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
- Reason
- Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Classification
- Class I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-25
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a95c1b3a-e3f4-413a-86dd-43c9b627a310